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DOI . ORG {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. Hosting Providers
  14. CDN Services

We began analyzing https://link.springer.com/chapter/10.1007/978-3-319-78127-3_6, but it redirected us to https://link.springer.com/chapter/10.1007/978-3-319-78127-3_6. The analysis below is for the second page.

Title[redir]:
Stromal Cells in the Tumor Microenvironment | SpringerLink
Description:
The tumor microenvironment comprises a mass of heterogeneous cell types, including immune cells, endothelial cells, and fibroblasts, alongside cancer cells. It is increasingly becoming clear that the development of this support niche is critical to the continued...

Matching Content Categories {πŸ“š}

  • Education
  • Science
  • Health & Fitness

Content Management System {πŸ“}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of doi.org audience?

πŸ™οΈ Massive Traffic: 50M - 100M visitors per month


Based on our best estimate, this website will receive around 80,904,851 visitors per month in the current month.

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How Does Doi.org Make Money? {πŸ’Έ}

We can't figure out the monetization strategy.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Doi.org could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {πŸ”}

pubmed, google, scholar, cas, article, cancer, cell, cells, central, tumor, stromal, fibroblasts, growth, res, human, immune, breast, med, biol, nature, chapter, acad, sci, proc, natl, pancreatic, microenvironment, factor, nat, matrix, signaling, roberts, cancerassociated, rev, fibroblast, myofibroblasts, tumors, transforming, factorbeta, epithelial, activation, denton, development, metastasis, access, lung, tgfbeta, antibody, tissue, stroma,

Topics {βœ’οΈ}

bone-marrow-derived myofibroblasts contribute platelet-derived growth factor-aa anti-pd-l1 antibody mpdl3280a transforming growth factor-beta month download article/chapter myeloid-derived suppressor cells platelet-derived growth factor anti-pd-l1 immunotherapy anti-pd-l1 antibody autocrine wnt-pcp signaling elevated tgf-beta1 secretion alpha-smooth muscle actin stromal cell-derived factor-1 bone marrow-derived stroma epithelial stem-cell compartments elevated sdf-1/cxcl12 secretion nf-kappab-dependent manner fibroblast activation protein orchestrate tumor-promoting inflammation van der heijden cancer-induced stromal reaction anti-pd-1 antibody anti-pd-l1 tgf-beta secretion hepatocyte growth factor autocrine tgf-beta matrix architecture defines device instant download directly promotes angiogenesis fap-expressing carcinoma promote tumor growth connective tissue remodelling bone marrow results bone marrow contribution privacy choices/manage cookies immune-mediated eradication die cellularpathologie matrix metalloproteinase-9 triggers topalian sl human breast cells stem cell rev high cd8+/regulatory editor information editors mammary epithelial cells including immune cells pancreatic stellate cells adult pancreatic cells enhancing integrin signaling autocrine ccr7 signaling epithelial tumor cells

Questions {❓}

  • How does the extracellular matrix direct gene expression?
  • Inflammation and cancer: back to Virchow?

Schema {πŸ—ΊοΈ}

ScholarlyArticle:
      headline:Stromal Cells in the Tumor Microenvironment
      pageEnd:114
      pageStart:99
      image:https://media.springernature.com/w153/springer-static/cover/book/978-3-319-78127-3.jpg
      genre:
         Biomedical and Life Sciences
         Biomedical and Life Sciences (R0)
      isPartOf:
         name:Stromal Immunology
         isbn:
            978-3-319-78127-3
            978-3-319-78125-9
         type:Book
      publisher:
         name:Springer International Publishing
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Alice E. Denton
            affiliation:
                  name:Babraham Institute
                  address:
                     name:Lymphocyte Signalling and Development, Babraham Institute, Cambridge, UK
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Edward W. Roberts
            affiliation:
                  name:University of California San Francisco
                  address:
                     name:Department of Pathology, University of California San Francisco, San Francisco, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Douglas T. Fearon
            affiliation:
                  name:Cold Spring Harbor Laboratory, Weill Cornell Medical College
                  address:
                     name:Cold Spring Harbor Laboratory, Weill Cornell Medical College, New York, USA
                     type:PostalAddress
                  type:Organization
            type:Person
      keywords:Cancer-associated fibroblast, Tumor microenvironment, Stromal immunology, Immunotherapy
      description:The tumor microenvironment comprises a mass of heterogeneous cell types, including immune cells, endothelial cells, and fibroblasts, alongside cancer cells. It is increasingly becoming clear that the development of this support niche is critical to the continued uncontrolled growth of the cancer. The tumor microenvironment contributes to the maintenance of cancer stemness and also directly promotes angiogenesis, invasion, metastasis, and chronic inflammation. In this chapter, we describe on the role of fibroblasts, specifically termed cancer-associated fibroblasts (CAFs), in the promotion and maintenance of cancers. CAFs have a multitude of effects on the growth and maintenance of cancer, and here we focus on their roles in modulating immune cells and responses; CAFs both inhibit immune cell access to the tumor microenvironment and inhibit their functions within the tumor. Finally, we describe the potential modulation of CAF function as an adjunct to bolster the effectiveness of cancer immunotherapies.
      datePublished:2018
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
      context:https://schema.org
Book:
      name:Stromal Immunology
      isbn:
         978-3-319-78127-3
         978-3-319-78125-9
Organization:
      name:Springer International Publishing
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Babraham Institute
      address:
         name:Lymphocyte Signalling and Development, Babraham Institute, Cambridge, UK
         type:PostalAddress
      name:University of California San Francisco
      address:
         name:Department of Pathology, University of California San Francisco, San Francisco, USA
         type:PostalAddress
      name:Cold Spring Harbor Laboratory, Weill Cornell Medical College
      address:
         name:Cold Spring Harbor Laboratory, Weill Cornell Medical College, New York, USA
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Alice E. Denton
      affiliation:
            name:Babraham Institute
            address:
               name:Lymphocyte Signalling and Development, Babraham Institute, Cambridge, UK
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Edward W. Roberts
      affiliation:
            name:University of California San Francisco
            address:
               name:Department of Pathology, University of California San Francisco, San Francisco, USA
               type:PostalAddress
            type:Organization
      name:Douglas T. Fearon
      affiliation:
            name:Cold Spring Harbor Laboratory, Weill Cornell Medical College
            address:
               name:Cold Spring Harbor Laboratory, Weill Cornell Medical College, New York, USA
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Lymphocyte Signalling and Development, Babraham Institute, Cambridge, UK
      name:Department of Pathology, University of California San Francisco, San Francisco, USA
      name:Cold Spring Harbor Laboratory, Weill Cornell Medical College, New York, USA
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {πŸ”—}(457)

Analytics and Tracking {πŸ“Š}

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Libraries {πŸ“š}

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Mail Servers:

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CDN Services {πŸ“¦}

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